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Timothy, Standardized - 0268-3064-06 - (Timothy, Standardized)

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Drug Information of Timothy, Standardized

Product NDC: 0268-3064
Proprietary Name: Timothy, Standardized
Non Proprietary Name: Timothy, Standardized
Active Ingredient(s): 10000    [BAU]/mL & nbsp;   Timothy, Standardized
Administration Route(s): PERCUTANEOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Timothy, Standardized

Product NDC: 0268-3064
Labeler Name: ALK-Abello, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103058
Marketing Category: BLA
Start Marketing Date: 19971218

Package Information of Timothy, Standardized

Package NDC: 0268-3064-06
Package Description: 5 mL in 1 VIAL, MULTI-DOSE (0268-3064-06)

NDC Information of Timothy, Standardized

NDC Code 0268-3064-06
Proprietary Name Timothy, Standardized
Package Description 5 mL in 1 VIAL, MULTI-DOSE (0268-3064-06)
Product NDC 0268-3064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Timothy, Standardized
Dosage Form Name SOLUTION
Route Name PERCUTANEOUS
Start Marketing Date 19971218
Marketing Category Name BLA
Labeler Name ALK-Abello, Inc.
Substance Name PHLEUM PRATENSE POLLEN
Strength Number 10000
Strength Unit [BAU]/mL
Pharmaceutical Classes Standardized Pollen Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Pollen [Chemical/Ingredient],Allergens [Chemical/Ingredient]

Complete Information of Timothy, Standardized


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